Canonical Allele Identifier: CA216976449
Gene: MUC2 HGNC NCBI

Linked Data

dbSNP Id: rs371816270
gnomAD v2: 11-1075491-A-C
gnomAD v3: 11-1075491-A-C
gnomAD v4: 11-1075491-A-C
MyVariant Identifiers: chr11:g.1075491A>C (hg19) chr11:g.1075491A>C (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.1075491A>C , CM000673.2:g.1075491A>C GRCh38
NC_000011.9:g.1075491A>C , CM000673.1:g.1075491A>C GRCh37
NC_000011.8:g.1065491A>C NCBI36
NG_051929.1:g.5617A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000361558.7:n.104-160A>C
ENST00000675028.1:c.77-160A>C ENSP00000502432.1:n.77-160A>C
NM_002457.3:c.77-160A>C NP_002448.3:n.77-160A>C
NM_002457.4:c.77-160A>C NP_002448.4:n.77-160A>C
Search 100 bp 5'
Search 100 bp 3'